Targeted exomes reveal simultaneous MFN2 and GDAP1 mutations in a severe Charcot‐Marie‐Tooth disease type 2 phenotype by Anghelescu, C, Francou, B, Cardas, R, Guiochon-Mantel, A, Aubourg, P, Servais, L, Gidaro, T

Autosomal recessive ataxias: a new gene - aprataxin - responsible for ataxia-ocular apraxia 1, and a new locus on 9q34 by Moreira, M, Klur, S, Barbot, C, Tachi, N, Bomont, P, Watanabe, M, Shoji, M, Warter, J, Aubourg, P, Durr, A, Nemeth, A, Amouri, R, Hentati, F, Alurkar, A, Divekar, D, Mendoca, P, Sequeiros, J, Coutinho, P, Koenig, M

Senataxin, the ortholog of a yeast RNA helicase, is mutant in ataxia-ocular apraxia 2. by Moreira, M, Klur, S, Watanabe, M, Németh, A, Le Ber, I, Moniz, J, Tranchant, C, Aubourg, P, Tazir, M, Schöls, L, Pandolfo, M, Schulz, J, Pouget, J, Calvas, P, Shizuka-Ikeda, M, Shoji, M, Tanaka, M, Izatt, L, Shaw, C, M'Zahem, A, Dunne, E, Bomont, P, Benhassine, T, Bouslam, N, Stevanin, G

Nonlinear laser spectroscopy by Atkins, C, Hancock, G, Zacharias, H, Beverini, N, Galli, M, Inguscio, M, Strumia, F, Bionducci, G, Bloomfield, L, Gerhardt, H, Hänsch, T, Boulnois, J, Aubourg, P, Van Lerberghe, A, Agrawal, G, Boyd, R, Harter, D, Chen, H, Erbert, G, Garrett, W, Payne, MG, Ferrell, W, Miller, J, Compton, R, Greenland, P